Middle ear primary tumors are rare. The middle era adenoma (MEA) is an infrequent entity with nonspecific clinical, audiologic, otoscopic and imaging findings. Definitive diagnosis is based on histological and immunohistochemical examination and the election treatment is the complete surgical removal of the lesion. We present a case of a middle ear neoplasm recently diagnosed and treated in our institution.from the middle ear mucosa that can have exocrine and/or neuroendocrine differentiation. It was first described in 1976 by Hyams & Michaels et al. [2], and later that year by Derlacki B et al. [3]. The clinical, otoscopic, audiologic and imaging findings are nonspecific. Definitive diagnosis is based on histological and immunohistochemical examination [1][2][3][4][5][6][7][8][9][10]. We report the case of a 48-year old man who was diagnosed and recently treated in our institution.
Case ReportIn October 2010, a 48-year old man presented at our otorhinolaryngology department with a 3-month history of right hearing loss, tinnitus and aural fullness. The otoscopy revealed a gray-white nonpulsatile poster superior retro tympanic mass with intact tympanic membrane (Figure 1). The hearing test confirmed a mild conductive hearing loss. A high-resolution temporal CT showed a well-circumscribed soft-tissue mass in the epitympanic area that was embedded in the ossicles without evidence of bone erosion (Figure 2). MRI revealed a middle ear mass with low intensity on T1weighted images, high intensity on T2-weighted images, and enhancement after administration of gadolinium.In January 2011, the patient underwent a right post auricular canal wall down mastoidectomy. A polypoid, fibrotic lesion was found in the middle ear cavity. It was located in the epitympanum and had firm adherences to the suprapiramydalis tympanic sinus. There was no involvement of the facial nerve. Even if the ossicles were embedded in the tumor, there was no ossicular chain erosion, but the incus was fractured. The intraoperative frozen study was not conclusive. A total excision of the lesion was performed and the head of the malleus and incus were removed. There were no major postoperative complications and the patient was discharged 24 hours after the procedure.Histologic examination of the excised tumor showed an epithelial neoplasm predominantly composed of cuboidal-tocolumnar cells with eosinophilic cytoplasm and round to oval nuclei. The cells were disposed forming trabecular, glandular and solid patterns (Figure 3). The histological morphology of the tumor was informed as compatible with MEA. A posterior immunohistochemical evaluation showed positivity for enolase, synaptophysin, vimentin, protein S100, cromogranin and cytokeratin. These findings confirmed the diagnosis of a MEA with neuroendocrine differentiation (Figure 4). The patient is currently disease free.